01 1H. Lundbeck AS
01 1Denmark
01 1Inactive
01 1Blank
01 1Blank
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21844
Submission : 2008-09-29
Status : Inactive
Type : II
A Tedatioxetine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tedatioxetine Hydrobromide, including repackagers and relabelers. The FDA regulates Tedatioxetine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tedatioxetine Hydrobromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tedatioxetine Hydrobromide supplier is an individual or a company that provides Tedatioxetine Hydrobromide active pharmaceutical ingredient (API) or Tedatioxetine Hydrobromide finished formulations upon request. The Tedatioxetine Hydrobromide suppliers may include Tedatioxetine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tedatioxetine Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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